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Evening Primorose Oil Versus Misoprostol in Cervical Preparation Before Operative Hysteroscopy

NCT07641595 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 230

Last updated 2026-06-11

No results posted yet for this study

Summary

This study aimed to compare the efficacy of misoprostol versus intravaginal Evening Primrose Oil capsule as a cervical ripening agent prior to operative hysteroscopy.

Conditions

  • Evening Primorose Oil
  • Misoprostol
  • Cervical Preparation
  • Hysteroscopy

Interventions

OTHER

Primorose Oil

Patients received evening Primorose Oil.

OTHER

Misoprostol

Patients received Misoprostol.

Sponsors & Collaborators

  • Sohag University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-11-12
Primary Completion
2026-05-21
Completion
2026-05-21

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07641595 on ClinicalTrials.gov